| Literature DB >> 1698933 |
G Nonaka1, I Nishioka, M Nishizawa, T Yamagishi, Y Kashiwada, G E Dutschman, A J Bodner, R E Kilkuskie, Y C Cheng, K H Lee.
Abstract
Nine tannins, including gallo- and ellagitannins, were evaluated as potential inhibitors of HIV replication. 1,3,4-Tri-O-galloylquinic acid [1], 3,5-di-O-galloyl-shikimic acid [2], 3,4,5-tri-O-galloylshikimic acid [3], punicalin [6], and punicalagin [7] inhibited HIV replication in infected H9 lymphocytes with little cytotoxicity. Two compounds, punicalin and punicacortein C [8], inhibited purified HIV reverse transcriptase with ID50 of 8 and 5 microM, respectively. Further studies with H9 lymphocytes indicated that chebulagic acid [5] and punicalin did not inactivate virus directly. However, 1,3,4-tri-O-galloylquinic acid and 3,5-di-O-galloylshikimic acid were more effective inhibitors under those conditions. All tannins appear to inhibit virus-cell interactions. Thus, inspite of their anti-RT activity, the mechanism by which tannins inhibit HIV may not be associated with this enzyme.Entities:
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Year: 1990 PMID: 1698933 DOI: 10.1021/np50069a008
Source DB: PubMed Journal: J Nat Prod ISSN: 0163-3864 Impact factor: 4.050